Investigator

Jin Hwi Kim

Catholic University of Korea

JHKJin Hwi Kim
Papers(5)
Gynecologic oncology …Collision Tumor of th…Tumour budding in pre…Primary signet ring c…Major clinical advanc…
Collaborators(10)
Jung-Yun LeeKwangil YimSung Jong LeeYoo-Young LeeDong Hoon SuhJeong-Yeol ParkJi Geun YooChan Joo KimTiara Bunga Mayang Pe…Yeon‐Sil Kim
Institutions(6)
Catholic University O…Yonsei UniversitySungkyunkwan Universi…Seoul National Univer…University Of UlsanRumah Sakit Umum Pusa…

Papers

Tumour budding in pretreatment cervical biopsies: a prognosticator for personalised therapy in the era of precision oncology

Aims Tumour budding (TB) is a noteworthy morphologic indicator for tumour microenvironment (TME) especially because it is detectable with routine haematoxylin and eosin (H&E) staining. Its prognostic relevance has been demonstrated across various cancers, but its significance in pretreatment biopsy specimens of cervical cancer is unknown. This is the first study to investigate the prognostic value of TB in pretreatment cervical biopsy. Additional TME features identifiable with H&E such as cell nest size (CNS) were evaluated. Methods and results A retrospective review was conducted on the 2018 International Federation of Gynaecology and Obstetrics (FIGO) stage IIVA cervical cancer patients ( N  = 182) who had completed standard treatment. In multivariate analysis, TB (hazard ratio [HR], 2.06) and CNS (HR, 2.16) independently predicted overall survival. While TB (AUC, 0.7065) slightly outperformed CNS (AUC, 0.6975) in discriminating overall survival, the combination of TB and CNS demonstrated the highest performance (AUC, 0.7192) in time‐dependent receiver operating characteristic analysis. Conclusions This study is the first to suggest TB in pretreatment biopsy specimens as a reliable morphologic prognosticator in cervical cancer. TME features may enhance precision oncology by offering insights into the individual tumour biology. The fact that these morphologic features are available from routine H&E slides, reserving immunohistochemistry or molecular analysis for indeterminate cases, is of particular value in low‐resource settings where the burden of cervical cancer is most significant.

9Works
5Papers
19Collaborators
Uterine Cervical NeoplasmsPrognosisTumor MicroenvironmentOvarian NeoplasmsUterine NeoplasmsCarcinoma, Signet Ring CellNeoplasm Recurrence, Local

Positions

Researcher

Catholic University of Korea